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Class Action Lawsuit Heartburn Medication

Types Of Cancer Linked To Zantac

Zantac Litigation – Is it a class action or individual lawsuits?

People who took contaminated Zantac and ranitidine-containing drugs are filing lawsuits for 12 types of cancer, including stomach, intestine and bladder cancer. Here is a full list of cancer types and the associated symptoms.

Type of Cancer

Each Zantac user’s cancer risk will depend on a number of factors, including:

  • The level of NDMA in the Zantac and/or ranitidine products they used
  • The length of time they used NDMA-containing Zantac
  • Individual health conditions

At this time, neither the U.S. Food and Drug Administration nor Zantac manufacturers have estimated the true cancer risk of Zantac. However, the FDA has estimated the cancer risk for NDMA-contaminated valsartan, a blood pressure drug. The agency determined that one additional cancer case would occur for every 8,000 people who took the drug for four years. It is unknown if Zantac would have a similar outcome.

According to Valisure’s data, Zantac contains enough carcinogen to cause cancer in lab animals.

A doctor can help estimate a person’s individual risk and appropriate level of vigilance in watching for signs of cancer. If you develop cancer after taking Zantac, our attorneys can determine if you are eligible to file a lawsuit.

Damages Available For Defective Drugs

After sustaining a serious injury or illness from a defective drug, you may be left with costly medical bills and feeling overwhelmed.

If you have a valid case, you may be able to pursue compensation for the damages you have suffered as a result of a dangerous drug. However, the amount and type of damages will depend on your individual circumstances. These could include compensation for economic and non-economic damages, such as:

  • Medical expenses
  • Pain and suffering
  • Loss of enjoyment of life

These are just some damages that may be available to victims of defective drugs. It is in your best interest to work with an experienced attorney, as proving the value of these losses and can be challenging. Our legal team can discuss your eligibility to pursue compensation in a free, no obligation consultation.

Complete our Free Case Evaluation form now.

Why Has Zantac Been Recalled

In a broad sense, the ultimate purpose of any product recall is to help improve consumer safety by removing the products from shelves. In this case, the recall serves to reduce the risk of exposure to cancer-causing substances found in Zantac and ranitidine. For this reason, you should immediately cease any Zantac consumption, and report any retailers who are still selling or distributing Zantac or any other dangerous drugs.

Also Check: What Is Safe To Take For Heartburn During Pregnancy

Science Connecting Zantac With Production Of Ndma

While we anticipate learning more about the connection between Zantac use and cancer from the various manufacturers as pending Zantac lawsuits move through the discovery phases of litigation, we know the following in terms of the correlation between the ingestion of Zantac and the bodies production of NDMA.

The science strongly supports that Zantac causes cancer.

  • National Cancer Institute: In 2004, the Center published a study that linked antacids and ranitidine to the development of bladder cancer.
  • Pottegard Study: This study examined men and women who took 150 mg tablets of ranitidine and examined their urine composition 24 hours before and after use. The study found NDMA levels in urine to be 47,600 ng /person. The equivalent of nearly 500 times higher than the FDA’s acceptable dose level.
  • Valisure: This pharmaceutical research company found an enzyme in the body that manufactures high levels of NDMA. The findings were concerning enough that they brought their findings to the attention of the FDA in September 2019.
  • Emery Pharma: In January 2020, the company filed a petition with the FDA finding that high levels of NDMA developed when ranitidine was exposed to heat .

The Dangers Of Nexium Prilosec And Prevacid

Proton Pump Inhibitors May Increase Risk of Developing ...

Dr. Oz: You know the names: Prilosec, Prevacid and, of course, the little purple pill Nexium. But now there are growing concerns that billions of people are taking these medicines needlesslytriggering dangerous side effects.

Source: foxnews.com/health/2016/04/25/more-evidence-links-heartburn-drugs-to-serious-kidney-problems.html

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Lawsuits Prilosec Nexium Prevacid

Many people have been harmed by their use of popular heartburn medications. The issue is that the drug maker did not adequately provide information to consumers about serious adverse side effects that taking these drugs could cause. The manufacturer knew about the hidden risks, but deliberately adjusted their warning labels and marketing efforts to hide that information and to keep sales and profits high.

As a result of this negligent behavior that caused personal injury to many PPI drug users, a large number of class action lawsuits and individual lawsuits have been filed against the drug manufacturers. One large worldwide business, AstraZeneca, has already paid out millions of dollars in damages to plaintiffs.

How We Created Our Zantac Ndma Exposure Chart

We used several pieces of information to construct the NDMA exposure chart above. First, we needed to know exactly how much NDMA was found in Zantac. There are two potential sources for this information:

  • Valisure DataValisure is an independent pharmacy. It was the first to raise the alarm about NDMA in Zantac. The company’s test results showed NDMA ranging from about 300,000 to 3,000,000 nanograms per Zantac tablet.
  • FDA DataIn response to a citizen petition from Valisure, the FDA performed its own tests. The FDA tests found unacceptable levels of NDMA in some products. NDMA levels ranged from 0 to 860 nanograms per tablet.

For our chart calculations, we chose to use the FDA’s data. Since the FDA levels were lower, this provides a conservative estimate of NDMA exposure.

To calculate NDMA exposure over time, we assumed a person would take the maximum daily dose. We multiplied the amount of NDMA found in recalled Zantac by the number of days indicated in each chart column.

To provide reference, we also calculated the amount of NDMA a person could ingest “safely.” We used the FDA’s maximum daily exposure level for NDMA . We multiplied this amount by the number of days in each chart column. It is represented by the small blue portion of each exposure bar.

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Food And Drug Administration Warns Of Cancer Risk With Zantac

Zantac is amongst the most popular and widely used OTC medications to relieve heartburn and gastroesophageal reflux.

Zantac belongs to the class of drugs known as H2 blockers, which decrease acid levels in the stomach.

In September 2019, the U.S. Food and Drug Administration issued a warning to consumers and healthcare professionals that laboratory tests revealed some ranitidine products to be contaminated with high levels of the suspected carcinogen called N-Nitrosodimethylamine NDMA, which is believed to be associated with an increased risk of a certain type of cancer.

The agency has since declared the NDMA levels found in these products to be “unacceptably high.”

According to FDA reports, exposure to significant amounts of NDMA can cause cancer in the liver, gastrointestinal tract, stomach, and colon and is known to damage the liver.

Are Nexium And Prilosec The Same Drug

Class Action Lawsuit Filed To Reopen Rental Relief Program

Esomeprazole is a mirror drug, meaning that is extremely similar to omeprazole , just like the left hand is the mirror image of the right hand. Technically they could be considered the same drug. Shortly after Prilosecs patent ended, however, AstraZeneca obtained the FDAs approval to market Nexium as a new drug just before the market was flooded with generic medications.

Many speculated that the pharmaceutical giant manufactured the new medication in order to maintain their revenues, since in the early 2000s Prilosec was the top-selling prescription medicine in the U.S., with yearly sales of $4.1 billion.

Esomeprazole and other PPIs are among the most overprescribed medications in the entire world, and theyre also grossly overpriced, especially in the United States. According to the American Society of Health-System Pharmacists, generic omeprazole is sold at about $1 per single dose, while esomeprazoles price is usually 7 to 15 times higher.

Dr. Marcia Angell, the former editor-in-chief of the New England Journal of Medicine, accused AstraZeneca of distorting the results of the studies that allegedly demonstrated esomeprazoles superiority over omeprazole to artificially overcharge the American consumers.

Also Check: What Medication To Take For Heartburn

Get A Prilosec Kidney Damage Lawsuit Started Today

If you took Prilosec or other PPI’s and later were diagnosed with kidney damage, chronic kidney disease, kidney failure or any other renal disease or failure, then call us and let us start investigating your potential claim or lawsuit against the makers of these products. This is NOT a medical malpractice lawsuit against any doctor, but rather product liability lawsuit against the makers of these over the counter heartburn medicines. At no time will you ever be sent a bill from our law firm. All cases are handled on a contingency fee basis.

No Fees or Expenses Charged Unless a Recovery is Made For You.

Talk to David Willis, a Board Certified Personal Injury Trial Lawyer that has been practicing for 30+ years. Willis has achieved The Highest Top Peer Review Ratings and is licensed in Texas & New York and is currently investigating and assisting clients in Nexium and Prilosec Kidney Damage Lawsuits Nationwide. Fill out form to the right of this page or

Speak With An Experienced Nyc Zantac Lawyer Today

If you face a cancer diagnosis after years of using heartburn medication such as Zantac, there may be a link between that medicine and your current health condition. The Jacob Fuchsberg Law Firm offers compassionate and thorough legal representation for those personally injured in all five boroughs of New York City and throughout the tri-state area of New York, New Jersey, and Connecticut.

Contact us or call to schedule a free case evaluation.

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Joseph L Galimidi Sues Sanofi For Breast Cancer

Florida resident Joseph L. Galimidi was one of the first to file an individual Zantac lawsuit in the United States against Sanofi on Sept. 13, 2019. Galimidi had been taking Zantac since 2009 and developed breast cancer, which is rare in men, in 2013.

He demands compensation for his injuries, pain and suffering.

Despite their knowledge of the risks of cancer associated with Ranitidine and Zantac Defendants continued to represent that Ranitidine products, including Zantac, did not pose any risks of cancer or other serious health conditions. Galimidi v. Sanofi et al.

While his heartburn was healed, Zantac laden with N-Nitrosodimethylamine , a probable human carcinogen wreaked havoc in his body and led to his breast cancer, Galimidis complaint said.

During the time Zantac and other ranitidine products have been sold in the United States, there have been reports of cancers linked to Zantac. Galimidi argues Sanofi had plenty of time to study the link and warn the public, but it did not.

Does Zantac Cause Cancer

Class Action Filed over Zantac and Cancer Risk

The higher levels of NDMA impurities in Zantac medications are linked with an increased cancer risk in humans. The U.S. Food and Drug Administration has released several advisory notices alerting the public of NDMA impurities present in Zantac and ranitidine medications. NDMA has been described as a known carcinogen in test animals, and humans may be particularly sensitive to NDMA exposure.

The FDA sets acceptable thresholds for NDMA daily intake at below 100 nanograms. Alarmingly, studies indicate that just one 150 mg dose of Zantac may contain upwards of 2.5 million nanograms of NDMA.

Also, newer FDA testing reveals that NDMA impurities in Zantac can increase over time as the products are stored . Thus, older Zantac products may contain even more NDMA, further increasing cancer risks for consumers. A knowledgeable attorney could help you understand the link between Zantac and cancer.

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What Type Of Cancer Does Zantac Cause

NDMA, Zantac, and ranitidine have a history of being associated with several types of primary cancers in humans. These include:

  • Breast cancer
  • Bladder cancer
  • Liver cancer and other cancers

Besides these major cancer risks, Zantac side effects can also include headaches, abdominal pain, nausea or vomiting, and other conditions. There are also health concerns associated with infants, as Zantac was commonly prescribed to babies for acidic stomach and other conditions.

If you or a loved one have been diagnosed with any of these types of cancer after using Zantac, you should contact one of our injury attorneys. The lawyers at Childers, Schlueter & Smith, LLC are available for a no-cost, private consultation to discuss your legal options moving forward.

Research Linking Zantac To Ndma/higher Risk Of Cancer

It is important to note that while Sanofi and Boerhinger Ingelheim were producing and marketing Zantac, there was research showing a link between ranitidine and NDMA and a potentially increased risk of developing cancer.

In 2004, a study found those taking Zantac or Tagamet for peptic ulcers had an increased risk of developing bladder cancer.

A 2016 study done by Stanford University researchers found patients urine contained large amounts of NDMA. Ten healthy volunteers received 150 milligrams of Zantac and tests of their urine found 47,000 nanograms of NDMA the amount in their bodies may have been higher because it would have been metabolized before becoming urine.

Sanofi disputes the methods used in this study and cites a 2013 meta-analysis of the possible link between acid-suppressing drugs and gastric cancer, which said there is not a statistically significant association. However, this analysis did find acid-suppressing drugs are associated with a higher risk of gastric cancer.

Contact Gordon & Partners about a potential Zantac lawsuit.

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Get In Touch With An Experienced Zantac Attorney

The injuries caused by Zantac are affecting many consumers who might not know that they are entitled to legal recourse. At Childers, Schlueter & Smith, LLC, we understand the types of issues and challenges such conditions can cause, and are here to provide you compassionate, responsive legal guidance.

Our Zantac lawyers work tirelessly to get you on the right track towards justice and recovery for you and your loved ones. Contact us for an evaluation of your case. Starting the process is the first step towards regaining your life. We provide representation for clients all over the country with unparalleled experience and results.

How These Heartburn Drugs Can Damage Your Kidneys

Unemployed Workers Union Files Class Action Lawsuit

Proton pump inhibitors like Nexium┬«, Prilosec┬« and Prevacid┬« all treat heartburn, indigestion and acid reflux by reducing the amount of acid produced by the stomach. But doctors and researchers aren’t exactly sure why PPI’s are damaging the kidneys in the process.

Many scientists believe PPI’s cause magnesium levels to drop in patients, which often damages the kidneys. Other researchers believe that kidney function is damaged due to repeated occurrences of acute kidney inflammation — which proton pump inhibitors are linked to.

Continue reading…

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Recent Ranitidine And Zantac Recalls

  • 12/18/2019: Glenmark Pharmaceutical Inc. recalls prescription Ranitidine tablets
  • 11/19/2019: Precision Dose recalls Ranitidine oral solution, USP 150 mg/10 ml
  • 11/15/2019: Golden State Medical Supply recalls Ranitidine HCl 150mg and 300mg capsules
  • 11/8/2019: Amneal Pharmaceuticals recalls Ranitidine tablets, 150 mg and 300 mg, and Ranitidine syrup , 15 mg/ml
  • 11/8/2019: American Health Packaging recalls Ranitidine liquid unit dose cups
  • 11/6/2019: Aurobindo & DG Health recalls Ranitidine
  • 10/25/2019: Novitium Pharma recalls Ranitidine Hydrochloride capsules 150 mg and 300 mg
  • 10/25/2019: Lannett Company, Inc. recalls Ranitidine syrup , 15mg/ml
  • 10/23/2019: Dr. Reddys, Kroger, Walgreens, and others recall Ranitidine tablets & capsules
  • 10/23/2019: Perrigo Company recalls Ranitidine
  • 10/22/2019: Sanofi recalls all Zantac OTC products (in the US
  • 9/25/2019: Apotex Corp. recalls 75mg and 150mg Ranitidine tablets
  • 9/23/2019: Sandoz Inc. recalled Ranitidine Hydrochloride capsules

Carcinogen In Zantac: What Is Ndma

NDMA is a contaminant that is known to potentially cause cancer. According to the Environmental Protection Agency, NDMA was used in the past for rocket fuel, but the chemical has been discontinued after high amounts of the substance were detected in the environment. Today NDMA is only used for research purposes, but it can also be released into the environment due to industrial pollution stemming from certain types of manufacturing. NDMA is also a byproduct of the chlorination of drinking water and wastewater. It isnt entirely clear how Zantac and other heartburn products became contaminated with NDMA, but the FDA is conducting an investigation. NDMA generally causes cancer only after high exposure or after exposure for a long period of time. Have you been taking heartburn medication for some time? Do you have cancer or do you have a family member who has cancer? You may be able to join a growing number of people considering pursuing a lawsuit against the makers of Zantac.

The Zantac mass tort lawyers at Madalon Law may be able to assist you with your case. Contact us today for a case review and to learn more about the next steps you may be able to take. It is predicted that many families and individuals may soon pursue class action lawsuits against the makers of these kinds of heartburn drugs.

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Learn More Aboutzantac Lawsuits

Side effects of Zantac may increase the risk of cancer, due to chemical impurities found in the heartburn drug.

While the FDAs permissible daily intake limit for NDMA is 96 ng, the complaint indicates that consumers taking a typical eight-week course of Zantac to treat peptic ulcer disease may be exposed to more than 280,000,000 ng of NDMA, and users taking a 150mg maintenance dose of Zantac daily are exposed to 889,000,000 ng over the course of a year.

Last month, the FDA issued warnings about the risk of the cancer-causing chemicals in Zantac, which has led to the widely used heartburn drug to be removed from many store shelves nationwide, and growing concerns among consumers about the long-term cancer risk they may now face.

NDMA has been a focus of FDA attention over the past year, after the chemical was detected in the generic blood pressure drug valsartan, resulting in hundreds of valartan lawsuits brought by former users who indicate they developed liver cancer, colorectal cancer and other digestive tract cancers following long term exposure to the tainted drug.

Zantac has been on the market since 1983, and was the first blockbuster drug to have sales surpass $1 billion per year. The lawsuit indicates that these sales were only possible due to a deception perpetrated by the drug makers, which may have caused unnecessary exposure to NDMA for years.

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